# Famotidine

NDC: 68071-4197
Generic name: Famotidine
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20010416

FDA application: ANDA075805

## Active ingredients

- FAMOTIDINE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-4197"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-4197
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=60cd0973-f74e-2b70-e053-2a91aa0a4361